Basic information Safety Supplier Related

PENTAERYTHRITOL TRICHLOROHYDRIN

Basic information Safety Supplier Related

PENTAERYTHRITOL TRICHLOROHYDRIN Basic information

Product Name:
PENTAERYTHRITOL TRICHLOROHYDRIN
Synonyms:
  • 3- CHLORO-2,2-BIS(CHLOROMETHYL)-1-PROPANOL
  • 3-CHLORO-2,2-DICHLOROMETHYLPROPANOL
  • PENTAERYTHRITOL TRICHLOROHYDRIN
  • 2,2-bis(chloromethyl)-3-chloro-1-propanol
  • Pentaerythrityl trichlorohydrin
  • 3-Chloro-2,2-bis(chloromethyl)propan-1-ol
  • 1-Propanol,3-chloro-2,2-bis(chloromethyl)-
  • 3-Chloro-2,2-bis(chloromethyl) propan-1-ol (Pentaerythrityl trichlorohydrin)
CAS:
813-99-0
MF:
C5H9Cl3O
MW:
191.48
Mol File:
813-99-0.mol
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PENTAERYTHRITOL TRICHLOROHYDRIN Chemical Properties

Melting point:
80 °C
Boiling point:
274.39°C (rough estimate)
Density 
1.4096 (rough estimate)
refractive index 
1.5300 (estimate)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
13.83±0.10(Predicted)
InChI
InChI=1S/C5H9Cl3O/c6-1-5(2-7,3-8)4-9/h9H,1-4H2
InChIKey
VRWHPVMGJTYPLS-UHFFFAOYSA-N
SMILES
C(O)C(CCl)(CCl)CCl
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Safety Information

HS Code 
2905599890
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PENTAERYTHRITOL TRICHLOROHYDRIN Usage And Synthesis

Synthesis

115-77-5

813-99-0

The general procedure for the synthesis of 3-chloro-2,2-dichloromethylpropan-1-ol from pentaerythritol was as follows: pentaerythritol (15 g, 0.11 mol) was dissolved in pyridine (27 ml) and heated to 65 °C. Thionyl chloride (24.7 ml, 0.33 mol) was added slowly and dropwise over a period of 4 h. The temperature of the reaction was controlled to be between 65°C and 95°C. After completion of the reaction, the reaction mixture was continued to be stirred at 50 °C for 18 hours. Subsequently, the reaction solution was heated to 120 °C-130 °C for concentration and then cooled to room temperature. The concentrated reaction solution was slowly poured into ice water (75 ml) and stirred for 30 minutes. The resulting solid product was collected by filtration, washed well with water and dried to give 3-chloro-2,2-bis(chloromethyl)propan-1-ol (15.4 g, 73% yield).

References

[1] Patent: KR101592370, 2016, B1. Location in patent: Paragraph 0204; 0205; 0206; 0207
[2] Australian Journal of Chemistry, 1988, vol. 41, # 12, p. 1953 - 1962
[3] Patent: US2835709, 1955,
[4] Mededelingen van de Koninklijke Vlaamse Academie voor Wetenschappen, Letteren en Schone Kunsten van Belgie, Klasse der Wetenschappen, 1940, vol. 2, # 5, p. 3,16
[5] Patent: US2835709, 1955,

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